Transparent article made of pvc graft copolymers

ABSTRACT

The invention relates to a method for producing vinyl chloride graft copolymers by emulsion polymerization and to a method for producing mixtures of said graft copolymers. The invention also relates to transparent molded bodies produced using the claimed graft copolymers or mixtures thereof.

The invention relates to a method for preparing vinyl chloride graftcopolymers by emulsion polymerization, and to a method for producingblends of such graft copolymers. The invention also relates totransparent moldings (i.e. molded articles) manufactured by using thegraft copolymers and their blends, respectively, according to theinvention.

Plasticized polyvinyl chloride (PVC) does not belong to the group ofthermoplastic elastomers (TPE) although it has TPE properties (PVCHandbook, Charles E. Wilkes, James W. Summers, Charles AnthonyDaniels—2005, page 14). Due to the low costs for the raw materials, themultifaceted processing properties and the good product features ittakes a special position among the thermoplastic elastomers. PlasticizedPVC shows very good stretchability and tensile strength due to theformation of microcrystallites and the dipole-dipole interactionsbetween chlorine and hydrogen atoms. By varying the percentage ofplasticizer in PVC the rigidity and flexibility of a product can beadjusted in a very easy manner. This has major logistic advantages forthe fabricator, since he can produce a plurality of products from only afew ingredients. Only the migration ability of the low-molecular weightplasticizer has to be considered a disadvantage. Due to migration of theplasticizer the material embrittles, which leads to a degradation of themechanical properties.

For many years, various oligomeric and polymeric plasticizers have beenemployed, which, due to their high molecular weights, show only littleto none tendency to migrate (Domininghaus-Kunststoffe, 7^(th) revisedand extended edition 2008). Known examples are copolymers consisting ofethylene-vinyl acetate-vinyl chloride (EVA-VC), ethylene-vinyl acetate(EVA, Levapren®), acrylonitrile-butadiene (NBR), styrene-butadiene(SBR), ethylene-vinyl acetate-carbon monoxide (Elvaloy®),styrene-butadiene-styrene (SBS, Kraton®) etc. The high-molecular weightplasticizers are blended with PVC or grafted with PVC in a suspensionpolymerization process. These products are only used for specialrequirements (low-temperature flexibility, low migration, fatresistance, etc.), since otherwise the disadvantages will prevail, suchas low plasticizing, more complex processing, inferior tear resistance,etc. To be considered a particularly serious drawback is the fact thatmoldings which were produced from a blend of PVC and the majority ofpolymeric plasticizers (elastomers) are opaque.

The PBA-g-PVC graft copolymers described in the prior art and preparedin emulsion or suspension processes can only be processed intotranslucent or opaque moldings.

Cross-linked polyacrylic esters (PAE) can be employed to improve thenotch impact strength of rigid PVC (EP 0472852). In DE 3803036 asuspension process is described which allows to obtain a PVC thatcontains 65 wt % of a cross-linked PAE. This product can be employed asan impact resistance modifier or as a polymeric plasticizer for PVC.

In EP 0647663 a method is described for producing thermoplasticallyelastomeric graft copolymerizates of PVC having cross-linkedpolyacrylates as a graft base or as a graft substrate.

In the prior art the only method known to us for producing transparentpolyacrylic ester-modified PVC articles using methods such as extrusion,injection molding or calendering, the usage of graft copolymers isdescribed which contain a certain percentage of polystyrene within thepolyacrylate phase. Due to its higher refractive index (n_(D) ²⁰=1.60),the content of polystyrene counterbalances the difference in therefractive indices of polybutyl acrylate and PVC(Dormininghaus-Kunststoffe, 7^(th) revised and extended edition 2008,chapter 2.1.2.2.1 Erhöhung der Schlagzähigkeit—Polyacrylate alsModifizierungsmittel für transparente PVC-Artikel, page 372). Due to thehigh glass transition temperature of polystyrene, this principle is onlysuitable for rigid PVC since the content of polystyrene outweighs theplasticizing effect of polyacrylates. Moreover, the UV and weatheringresistance of the PVC articles is impaired owing to the content ofpolystyrene.

Thus, it is an object of the invention to provide materials withoutadding external plasticizers (in various degrees of hardness Shore A 70to Shore D 80, if necessary), based on vinyl chloride, which can beprocessed into transparent films and molded articles.

An object of the present invention is a method for producing a vinylchloride graft copolymer by using emulsion polymerization, wherein thegraft copolymer contains a graft base and a grafted copolymer phase,which at least partially consists of vinyl chloride, comprising thesteps of:

-   a) Preparing a graft base by polymerizing monomers, wherein the    glass transition temperature T_(g) of the graft base is adjusted by    appropriately selecting the monomers to be used, and-   b) Grafting a copolymer phase onto the graft base prepared in a) by    using emulsion polymerization, thus obtaining a vinyl chloride graft    copolymer latex, wherein by appropriately selecting the monomers to    be used and the optionally used comonomers, the glass transition    temperature T_(g) of the grafted copolymer phase is adjusted in such    a way that the glass transition temperature T_(g) of the graft base    is lower than the glass transition temperature T_(g) of the grafted    copolymer phase, and-   c) Separating the vinyl chloride graft copolymer as a solid from the    vinyl chloride graft copolymer latex,    characterized in that by appropriately selecting the polymerization    conditions in step b) the average particle size of the vinyl    chloride graft copolymer is adjusted to less than 300 nm, preferably    less than 200 nm, particularly preferably less than 150 nm and most    preferably less than 100 nm.

In a systematic study it has been found that the particle size of thegraft copolymer prepared in an emulsion process has a great influence onthe transparency of molded articles produced therefrom. By reducing thediameter of the particles to below certain values the transparency of apress plate manufactured therefrom will be highly improved. This alsoapplies to vinyl chloride graft copolymers having a cross-linked graftbase and a non-cross-linked graft shell or having both a cross-linkedgraft base and a cross-linked graft shell.

The glass transition temperature T_(g) of the grafted copolymer phasetypically lies in the range of above 20 to 120° C. and/or the one of thegraft base in the range of −80 to 20° C. In a preferred embodiment ofthe invention the glass transition temperature T_(g) of the graftedcopolymer phase lies between 40 and 90° C., and the one of the graftbase between −60 and −20° C. The T_(g)'s of the grafted copolymer phaseand of the graft base result from the composition of the respectivelyused monomers.

The vinyl chloride graft copolymers are prepared in an emulsion process.In doing so, the graft base can be prepared by copolymerizing vinylcompounds. The grafted compound can be prepared from 60 to 100 wt % ofvinyl chloride, preferably 80 to 100 wt %, and from 0 to 40 wt % ofother polymerizable vinyl compounds, preferably 0 to 20 wt %.

In another preferred embodiment the graft base and/or the graftedcopolymer phase are cross-linked.

The emulsion polymerization is preferably carried out semi-continuously.In the preparation process of the graft base, water, initiators,monomers, emulsifiers and other additives can be pre-charged into areactor and partly added in small amounts. In a preferred embodiment,water and the total amount of emulsifier are pre-charged and both themonomers and the initiators are added. The feeding speed of theadditives is based upon the conversion speed. The duration of thepolymerization is adjusted to one to three hours by the amount of theinitiator employed. After the polymerization has ended, the graft baseis processed and pre-charged for the preparation of the graft copolymer.Vinyl chloride and, if applicable, other polymerizable vinyl compounds,are added within 10 min to 180 min. In a preferred embodiment, theamount of VC is divided into a portion to be pre-charged and a portionto be added. In the process, 5 to 20 parts of VC are pre-charged (atonce), then polymerized until the pressure drops, and then the additionof the residual amount of VC is started. The temperature is regulated toadjust the desired K-value. To speed up the polymerization, an initiatoris added simultaneously. An emulsifier can be added to increase thestability of the dispersion. The content of solids in the fullypolymerized dispersion lies between 20 and 60 wt %, and preferablybetween 30 and 55 wt %.

Suitable vinyl compounds for the graft base are, for example, acrylicacid esters or methacrylic acid esters (in brief: (meth)acrylic acidester). Also, butadiene, 2-chloro-butadiene, 1-butene, isoprene,vinylidene chloride, vinyl acetate, vinyl alkyl ether, etc. can be usedas vinyl compound.

For the grafting, preferably merely vinyl chloride is used. But it isalso possible to homo- or copolymerize (meth)acrylic acid esters, whichcontain 1 to 12 carbon atoms in the alkyl chain of the esterifiedlinear, branched or cyclic alcohol, such as methyl acrylate, ethylacrylate, propyl acrylate, butyl acrylate, t-butyl acrylate, pentylacrylate, isopentyl acrylate, cyclohexyl acrylate, ethylhexyl acrylate,methyl methacrylate, ethyl methacrylate, propyl methacrylate, butylmethacrylate, t-butyl methacrylate, pentyl methacrylate, isopentylmethacrylate, ethylhexyl methacrylate, cyclohexyl methacrylate, etc.

In step b) of the method according to the invention the copolymer phaseis typically grafted by emulsion polymerization using at least oneemulsifier, in which preferably 60 to 100 wt % of the emulsifier amountis pre-charged, based on the total amount of emulsifier.

The polymerization temperature in the process of preparing each of thegraft bases typically lies between 20 and 90° C., preferably between 60and 95° C.

The polymerization temperature in the process of preparing each of thegrafted copolymer phases typically lies between 45 and 90° C.,preferably between 55 and 70° C.

The percentage of the graft base is preferably 5 to 70 wt %, and thepercentage of the grafted copolymer phase is preferably 30 to 95 wt %,in each case based on the vinyl chloride copolymer.

Suitable ionic emulsifiers are alkyl sulfonates, aryl sulfonates, alkylsulfates, alkyl ether sulfates, fatty acid salts, diaryl sulfonates,etc. It is also possible to use non-ionic emulsifiers, such as alkylether alcohols having 2 to 20 carbon atoms in the alkyl chain and 1 to20 ethylene glycol units, fatty alcohols, etc., alone or in combinationwith ionic emulsifiers. The total amount of emulsifier used lies between0.1 to 5 wt %, based on the amount of monomers employed.

Suitable initiators are water-soluble peroxides, which form radicals bythermal decomposition alone or which can be caused to decompose incombination with a reducing agent and, if necessary, a catalyst. Theamount of the initiators employed usually lies between 0.01 and 0.5 wt%, based on the monomers employed.

In a preferred embodiment of the invention the graft base iscross-linked by copolymerization with one or more different monomersthat contain two or more non-conjugated ethylenically unsaturated doublebonds. Optionally, it is possible to additionally cross-link the graftedcopolymer phase by copolymerization with one or more different monomersthat contain two or more non-conjugated ethylenically unsaturated doublebonds.

In another preferred embodiment of the invention, a) both the graft baseand the graft shell will not be cross-linked, or b) the graft base willnot be cross-linked and the graft shell will be cross-linked.

Suitable compounds for cross-linking are diallyl phthalate, allylmethacrylate, allyl acrylate, ethylene glycol dimethacrylate, propyleneglycol dimethacrylate, butylene glycol diacrylate, trimethylene glycoldiacrylate, glycidyl methacrylate, glycidyl acrylate, etc.

In the method according to the invention, a vinyl chloride graftcopolymer-containing latex is obtained by way of emulsionpolymerization. The solid will be separated either by adding anelectrolyte, coagulation and mechanical separation methods such asfiltration, decantation, centrifugation of the latex, followed bydrying, or by spray drying.

In a particular embodiment of the invention at least two different vinylchloride graft copolymers are prepared independently of each other andmixed subsequently, giving a blend in which the at least two differentgraft copolymers differ from each other by their respective percentageweight distribution of the graft base and the grafted copolymer phase.

In a particular embodiment of the invention the steps a), b), and c) andthe blending are carried out in such a way that the blend contains:

-   A) one or more graft copolymers A, each containing 41 to 70 wt % of    graft base and 30 to 59 wt % of grafted copolymer phase, and/or-   B) one or more graft copolymers B, each containing 26 to 40 wt % of    graft base and 60 to 74 wt % of grafted copolymer phase, and/or-   C) one or more graft copolymers C, each containing 5 to 25 wt % of    graft base and 75 to 95 wt % of grafted copolymer phase,    wherein the blend contains at least two different graft copolymers    that are covered by A) and B), by B) and C), by A) and C), or at    least three different graft copolymers that are covered by A), B)    and C).

In a further preferred embodiment of the invention the steps a), b) andc) and the blending are carried out in such a way that a blend isobtained consisting of:

-   A) one or more graft copolymers A in an amount of 1 to 99 wt %,    based on the blend, each graft copolymer A containing    -   30 to 59 wt % of a grafted copolymer phase, at least partially        prepared from vinyl chloride, having a glass transition        temperature T_(g) in the range of above 20 to 120° C., and    -   41 to 70 wt % of a graft base having a glass transition        temperature T_(g) in the range of −80 to 20° C., and/or-   B) one or more graft copolymers B in an amount of 1 to 99 wt %,    based on the blend, each graft copolymer B containing    -   60 to 74 wt % of a grafted copolymer phase, at least partially        prepared of vinyl chloride, having a glass transition        temperature T_(g) in the range of above 20 to 120° C., and    -   26 to 40 wt % of a graft base having a glass transition        temperature T_(g) the range of −80 to 20° C., and/or-   C) one or more graft copolymers C in an amount of 1 to 99 wt %,    based on the blend, each graft copolymer C containing    -   75 to 95 wt % of a grafted copolymer phase, at least partially        prepared from vinyl chloride, having a glass transition        temperature T_(g) in the range of above 20 to 120° C., and    -   5 to 25 wt % of a graft base having a glass transition        temperature T_(g) in the range of −80 to 20° C., and/or-   D) further ingredients in an amount of 0 to 75 wt %, based on the    blend, wherein the blend contains at least 25 wt % of graft    copolymers that together meet at least two of the conditions A), B)    and C), and the total percentage of the ingredients covered by A),    B), C) and D) adds to 100%.

Also an object of the invention is a vinyl chloride graft copolymerprepared according to the method described above.

A further object of the invention is a blend that contains differentvinyl chloride graft copolymers prepared according to the methoddescribed above.

Also an object of the invention is an article prepared by using a vinylchloride graft copolymer prepared according to the method describedabove or by using a blend that contains different vinyl chloride graftcopolymers prepared according to the method described above.

Preferred articles according to the invention have a transmittance of atleast 65%, preferably of at least 75%, and particularly preferred of atleast 85%, and/or a haze value of at most 60, preferably of at most 50,and particularly preferred of at most 40.

Also an object of the invention is the use of a vinyl chloride graftcopolymer and the use of the blends described above for manufacturing anarticle, preferably for manufacturing films by way of extrusion and/orcalendering or for manufacturing molded articles by way of extrusion orinjection molding or other thermoplastic molding methods.

In the following examples the method according to the invention forpreparing graft copolymers of vinyl chloride, having a hightransparency, is described.

EXAMPLES Example 1 Graft Base

Into a 10-liter reactor with stirrer, 4156 g of deionized water, 0.4 gof allyl methacrylate, 78 g of butyl acrylate, 705.9 g of potassiummyristate (concentration: 5 wt %), and 0.720 g of potassiumperoxodisulfate were pre-charged and heated to 80° C. After the reactionhad started, adding of 784.3 g of a 0.3% aqueous solution of potassiumperoxodisulfate was carried out within 180 min. Simultaneously, 11.36 gof allyl methacrylate and 2263 g of butyl acrylate were added within 180min. After the addition had ended the reaction temperature wasmaintained for 60 min and the preparation was cooled down subsequently.

7911 g of the dispersion were obtained. The solid content was 29.8%, thesurface tension was 52.2 mN/m and the pH was 7.6. The averagevolume-based particle size (PSV) was 12 nm.

Graft Copolymer:

Into a 10-liter autoclave with a water-cooled double jacket and a paddleagitator, 1367 g of water, 332 g of a 5% solution of potassiummyristate, 3087 g of graft base, 4.32 g of diallyl phthalate and 1076 gof vinyl chloride were pre-charged and heated to 68° C. When thepolymerization temperature was reached, adding of potassiumperoxodisulfate and ascorbic acid was started. The adding speed wasadjusted in such a way that the difference between the interiortemperature and the supply temperature of the jacket cooling was about10° C. After the pressure had dropped by 4 bars, the preparation was setto cool and depressurized. The dispersion was discharged. The solidcontent of the dispersion was 30.7 wt %, the surface tension was 56.7mN/m, the pH was 7.7. The average volume-based particle size was 61 nm.The preparation was precipitated with calcium chloride and filtered bysuction filtration. The residue was dried at 30° C. in arecirculating-air dryer to a residual moisture of <0.3% and finelyground with a centrifugal mill (Retsch ZM 200). The PBA content wasdetermined to be 46.9 wt % by an oxygen analysis.

Example 2 Graft Base

The graft base of Example 1 was used.

Graft Copolymer:

Into a 10-liter autoclave with a water-cooled double jacket and a paddleagitator 2365 g of water, 387.3 g of a 5% solution of potassiummyristate, 2506 g of graft base, 6.347 g of diallyl phthalate and 1580 gof vinyl chloride were pre-charged and heated to 68° C. When thepolymerization temperature was reached, adding of potassiumperoxodisulfate and ascorbic acid was started. The adding speed wasadjusted in such a way that the difference between the interiortemperature and the supply temperature of the jacket cooling was about10° C. After the pressure had dropped by 4 bars, the preparation was setto cool and depressurized. The dispersion was discharged. The solidcontent of the dispersion was 30.5 wt %, the surface tension was 58.5mN/m, the pH was 8.0. The average volume-based particle size was 58 nm.The preparation was precipitated with calcium chloride and filtered bysuction filtration. The residue was dried at 30° C. in arecirculating-air dryer to a residual moisture of <0.3% and finelyground with a centrifugal mill (Retsch ZM 200). The PBA content wasdetermined to be 33 wt % by an oxygen analysis.

Example 3 Graft Base

The preparation of Example 1 was repeated. 7909 g of an aqueousdispersion were discharged. The solid content of the dispersion was 30wt %, the surface tension was 54.4 mN/m, the pH was 7.4. The averagevolume-based particle size was 12 nm.

Graft Copolymer:

3144 g of water, 387.3 g of a 5% solution of potassium myristate, 1400 gof graft base, 1906 g of vinyl chloride and 7.63 g of diallyl phthalatewere pre-charged and polymerized following Example 1. The dispersion wasdischarged. The solid content of the dispersion was 29.6 wt %, thesurface tension was 51.9 mN/m, the pH was 8.1. The average volume-basedparticle size was 56 nm. The preparation was precipitated with calciumchloride and filtered by suction filtration. The residue was dried at30° C. in a recirculating-air dryer to a residual moisture of <0.3% andfinely ground with a centrifugal mill (Retsch ZM 200). The PBA contentwas determined to be 19.2 wt % by an oxygen analysis.

Example 4 Graft Base

Into a 10-liter reactor with stirrer, 2642 g of deionized water, 0.80 gof diallyl phthalate, 77 g of butyl acrylate, 315.3 g of potassiummyristate (concentration: 1.85 wt %) and 0.714 g of potassiumperoxodisulfate were pre-charged and heated to 80° C. After the reactionhad started, adding of 1167 g of a 0.1% aqueous solution of ammoniumperoxodisulfate was carried out within 180 min. Simultaneously, 22.55 gof diallyl phthalate, 2233 g of butyl acrylate and 1009 g of a 1.85%potassium myristate solution were added within 180 min. After theaddition had ended, the interior reactor temperature was maintained for60 min and the preparation was cooled down subsequently. 7335 g of thedispersion were obtained. The solid content was 30.9%, the surfacetension was 54.4 mN/m and the pH was 8.3.

Graft Copolymer:

2144 g of water, 280 g of 5% potassium myristate solution and 3021 g ofgraft base were pre-charged and heated to 68° C. Then, 117 g of vinylchloride were added and further 1278 g of vinyl chloride were addedwithin 100 min. For the activation, a hydrogen peroxide solution and anascorbic acid solution were used. The adding speed was adjusted in sucha way that the difference between the interior temperature and thesupply temperature of the jacket cooling was about 10° C. After thepressure had dropped by 4 bars, the preparation was set to cool anddepressurized. The solid content of the dispersion was 28.8 wt %, thesurface tension was 54.9 mN/m, the pH was 7.5. The average volume-basedparticle size was 92 nm. The preparation was precipitated with calciumchloride and filtered by suction filtration. The residue was dried at30° C. in a recirculating-air dryer to a residual moisture of <0.3% andfinely ground with a centrifugal mill (Retsch ZM 200). The PBA contentwas determined to be 41.1 wt % by an oxygen analysis.

Example 5 Graft Base

Into a 10-liter reactor with stirrer, 1784 g of deionized water, 68.25 gof butyl acrylate, 0.35 g of allyl methacrylate, 411.8 g of potassiummyristate (concentration: 1 wt %), and 0.63 g of potassiumperoxodisulfate were pre-charged and heated to 80° C. After the reactionhad started, adding of 686 g of a 0.3% aqueous solution of potassiumperoxodisulfate was performed within 180 min. Simultaneously, 1980 g ofbutyl acrylate, 9.94 g of allyl methacrylate and 2059 g of a 1%potassium myristate solution were added within 180 min. After theaddition had ended, the interior reactor temperature was maintained for60 min and the preparation was cooled down subsequently. 6963 g of thedispersion were discharged, having a solid content of 29.6 wt %, thesurface tension was 56.4 mN/m and the pH was 8.1. The averagevolume-based particle size was 74 nm.

Graft Copolymer:

The preparation was prepared following Example 1. The solid content ofthe dispersion was 32.4 wt %, the surface tension was 48.8 mN/m, the pHwas 8.0. The average volume-based particle size was 131 nm. Thepreparation was precipitated with calcium chloride and filtered bysuction filtration. The residue was dried at 30° C. in arecirculating-air dryer to a residual moisture of <0.3% and finelyground with a centrifugal mill (Retsch ZM 200). The PBA content wasdetermined to be 50.0 wt % by an oxygen analysis.

The samples according to the invention can be processed to transparentpress plates. The samples according to the invention are characterizedin that both the graft base and the graft shell are non-cross-linked, orthat the graft base is non-cross-linked while the graft shell iscross-linked, or that the average particle size is below 150 nm whenboth the graft base and the graft shell are cross-linked, or when onlythe graft base is cross-linked while the graft shell isnon-cross-linked.

The Comparative Examples mentioned below give proof that such pressplates are opaque that were made from graft copolymers having a particlesize of greater than 150 nm, which have both a cross-linked graft baseand a cross-linked graft shell or which have a cross-linked graft baseand a non-cross-linked graft shell.

Comparative Example 1 Graft Base

Into a 10-liter reactor with stirrer, 1887 g of deionized water, 68.25 gof butyl acrylate, 0.35 g of allyl methacrylate, 308.8 g of potassiummyristate (concentration: 1 wt %), and 0.63 g of potassiumperoxodisulfate were pre-charged and heated to 80° C. After the reactionhad started, adding of 686 g of a 0.3% aqueous solution of potassiumperoxodisulfate was performed within 180 min. Simultaneously, 1980 g ofbutyl acrylate, 9.94 g of allyl methacrylate and 2059 g of a 1%potassium myristate solution were added within 180 min. After theaddition had ended, the interior reactor temperature was maintained for60 min and the preparation was cooled down subsequently. 6925 g of thedispersion were discharged, having a solid content of 29.6 wt %, asurface tension of 52.6 mN/m and a pH of 8.2. The average volume-basedparticle size was 135 nm.

Graft Copolymer:

The preparation was prepared following Example 1. The solid content ofthe dispersion was 28.3 wt %, the surface tension was 42.5 mN/m, the pHwas 8.4. The average volume-based particle size was 176 nm. Thepreparation was precipitated with calcium chloride and filtered bysuction filtration. The residue was dried at 30° C. in arecirculating-air dryer to a residual moisture of <0.3% and finelyground with a centrifugal mill (Retsch ZM 200). The PBA content wasdetermined to be 49.6 wt % by an oxygen analysis.

Comparative Example 2 Graft Base

Into a 10-liter reactor with stirrer, 1990 g of deionized water, 68.25 gof butyl acrylate, 0.35 g of allyl methacrylate, 205.9 g of potassiummyristate (concentration: 1 wt %), and 0.63 g of potassiumperoxodisulfate were pre-charged and heated to 80° C. After the reactionhad started, adding of 686 g of a 0.3% aqueous solution of potassiumperoxodisulfate was performed within 180 min. Simultaneously, 1980 g ofbutyl acrylate, 9.94 g of allyl methacrylate and 2059 g of a 1%potassium myristate solution were added within 180 min. After theaddition had ended, the interior reactor temperature was maintained for60 min and the preparation was cooled down subsequently. The averagevolume-based particle size was 180 nm.

Graft Copolymer:

The preparation was prepared following Example 1. The solid content ofthe dispersion was 26.3 wt %, the surface tension was 40.8 mN/m, the waspH 8.8. The preparation was precipitated with calcium chloride andfiltered by suction filtration. The residue was dried at 30° C. in arecirculating-air dryer to a residual moisture of <0.3% and finelyground with a centrifugal mill (Retsch ZM 200). The PBA content wasdetermined to be 52 wt % by an oxygen analysis. The average volume-basedparticle size was 224 nm.

Comparative Example 3 Graft Base

Into a 10-liter reactor with stirrer, 2134 g of deionized water, 68.29 gof butyl acrylate, 0.34 g of allyl methacrylate, 61.76 g of potassiummyristate (concentration: 1 wt %) and 0.63 g of potassiumperoxodisulfate were pre-charged and heated to 80° C. After the reactionhad started, adding of 686.3 g of a 0.3% aqueous solution of potassiumperoxodisulfate was performed within 180 min. Simultaneously, 1980 g ofbutyl acrylate, 9.94 g of allyl methacrylate and 2059 g of a 1%potassium myristate solution were added within 180 min. After theaddition had ended the interior reactor temperature was maintained for60 min the preparation was cooled down subsequently.

6998 g of an aqueous dispersion, having a solid content of 29.6 wt %, asurface tension of 47.9 mN/m and a pH of 8.3, were obtained. The averagevolume-based particle size was 272 nm.

Graft Copolymer:

Into a 10-liter autoclave with a water-cooled double jacket and a paddleagitator, 1515 g of water, 387 g of a 5% solution of potassiummyristate, 3705 g of graft base, 9.33 g of diallyl phthalate and 1227 gof vinyl chloride were pre-charged and heated to 68° C. When thepolymerization temperature was reached, adding of potassiumperoxodisulfate and ascorbic acid was started. The adding speed wasadjusted in such a way that the difference between the interiortemperature and the supply temperature of the jacket cooling was about10° C. After the pressure had dropped by 4 bars, the preparation was setto cool and depressurized. The dispersion was discharged. The solidcontent of the dispersion was 27.1 wt %, the surface tension was 38.8mN/m, the pH was 8.2. The preparation was precipitated with calciumchloride and filtered by suction filtration. The residue was dried at30° C. in a recirculating-air dryer to a residual moisture of <0.3% andfinely ground with a centrifugal mill (Retsch ZM 200). The PBA contentwas determined to be 56.6 wt % by an oxygen analysis. The averagevolume-based particle size was 336 nm.

Comparative Example 4 Graft Base

The same graft base as in Example 3 was used.

Graft Copolymer:

1299 g of water, 332 g of a 5% potassium myristate solution, 3176 ofgraft base and 1060 g of vinyl chloride were pre-charged and thenpolymerized based on Comparative Example 3. The dispersion wasdischarged. The solid content of the dispersion was 27.1 wt %, thesurface tension was 37.4 mN/m, the pH was 8.7. The preparation wasprecipitated with calcium chloride and filtered by suction filtration.The residue was dried at 30° C. in a recirculating-air dryer to aresidual moisture of <0.3% and finely ground with a centrifugal mill(Retsch ZM 200). The PBA content was determined to be 57.2 wt % by anoxygen analysis. The average volume-based particle size was 327 nm.

On a two-roll roller the powdered graft copolymers were processed andpressed into rolled sheets. In the following Table 1 the poly(butylacrylate) content, the degree of cross-linking, the particle sizes ofthe graft copolymers and the optical properties (transmittance, haze)are given.

Experimental Procedures:

Measurement of Particle Sizes:

The particle size distributions were measured with a Microtrac Blue-Waveof the S3500 series by Particle-Metrix. The valid measuring range liesbetween 0.01 and 2000 μm. For the measurement, a standard procedure fordispersions was created, where certain physical properties of thedispersion were given. Before measurement, three drops of Hellmanex® (byHellmanex-Analytics Inc.) were added to the deionized water inside thecirculation unit, using a disposable 3 ml pipette. The cleanliness ofthe measurement system was validated by a baseline measurement.Dispersion was added carefully to the sample unit until a loading factorof about 0.004 was reached. Normally, 1 or 2 drops of dispersion aresufficient. The measurement time was 30 s. Evaluation of the measurementis carried out automatically. The average volume-based particle size isused.

Two-Roll Rolling Mill (Including Processing Conditions and Recipe)

To determine mechanical values and optical properties, test samples haveto be provided. The preparation of the rolled sheets is performed underthe following conditions.

Recipe (spatula blend) 100 phr Polymer 1.5 phr BaZn stabilizer(Baerostab UBZ 171) 3.0 phr Epoxydated soy bean oil (Edenol D 81) 0.1phr Isotridecyl stearate (Loxiol G 40) 0.2 phr High-molecular weightmulti-part adhesive (Loxiol G 72) 0.1 phr Calcium stearate (Ceasit SW)

Rolling mill (made by Schwabenthan)

Roller material: chromed surfaces

Roller diameter: 150 mm

Speed ratio: 17/21 1/min

Roller temperature: 140° C.

Rolling time: 5 min

Execution:

In order to form a cohesive mass (sheet) the powder compound is placedonto the roller. After formation of the sheet, it is “cut” and “turned”for 3 min. Then set the thickness of the rolled sheet to 1.1 mm andcontinue to plasticize on the roller for further 2 min without cuttingand turning. When the specified rolling time is over, the rolled sheetis taken off.

Press

30-ton laboratory press (Werner & Pfleiderer URH 30)

Press area: 350×350 mm

Pressing plates: chromed surfaces

Pressing frame: 220×220×1.0 mm

Execution:

For making the press plates, the previously rolled sheets were cutcorresponding to the frame size used, inserted into the frame and placedinto the laboratory press together with the press plates that form theouter surfaces. The sheets are formed into a press plate under theconditions described below.

Press temperature: 150° C. LP press power: 30 bar LP pressing time: 2min HP press power: 200 bar HP pressing time: 3 min Removal temperature:40° C. Cooling pressure: 220 bar Cooling time: 8 min

Transmittance and Haze (Large-Angle Scattering)

In order to evaluate a film's transparency two values were considered:

-   -   the total transmittance (here: “transmittance”), which stands        for the ratio of transmitted light to incident light and which        depends on absorption properties and surface conditions    -   large-angle scattering (haze), which is a measure for        opaqueness.

Measurement:

The measurement of the transmittance and the determination of thelarge-angle scattering of the semi-finished products produced withrollers/presses is carried out with the transparency meter Haze-GardDual by Byk-Gardner Inc.

The sample to be measured is illuminated perpendicularly and thetransmitted light is photoelectrically measured in an integratingsphere. The perpendicularly transmitted light is measured in order toevaluate the transmittance, and the light that is scattered in an angleof 2° to the axis of irradiation is measured to evaluate the opaqueness(haze). The measurements are carried out according to ISO 13468. Thisguarantees that the measurement conditions are the same duringcalibration as well as during measurement.

TABLE 1 Overview: Test and Comparative Examples and Press Plates MadeTherefrom PBA Microtrac Thickness of content MV Shore Shore Press PlatesPatent Examples (wt %) (nm) Hardness A Hardness D (mm) Transmittance, %Haze Remarks Example 1 46.9 61 85 26 1.50 84 13.2 Graft base and Example2 33 58 97 46 1.68 80.7 6.92 graft shell cross- Example 3 19.2 56 97 591.74 74.8 9.06 linked and PSV Example 4 41.1 92 90 35 1.73 83.0 11.7<150 nm Example 5 50 131 87 31 1.56 78.4 13.0 Comparative 49.6 176 87 321.57 73.0 21.9 Comparative Example 1 Examples PSV ≧150 nm Comparative 52224 84 24 1.83 52.6 43.5 Example 2 Comparative 56.6 336 88 31 1.59 52.452.7 Example 3 Comparative 57.2 327 85 27 1.64 48.3 63.7 Example 4 BlendExample 1 29.6 94 59 1.67 75.4 16.4 0.75 Example 2 + 0.25 Example 3Blend Example 2 40 92 38 1.49 69.9 93.2 0.75 Example 1 + 0.25 Example 3Vinnolit VK 710 ca. 50 85 28 1.48 78.0 65.8 Competitive Vinnolit K 707 Eca. 50 79 25 1.81 53.9 68.8 product samples

The graft copolymers Vinnolit VK 710 and Vinnolit K707 E, having anacrylate content of about 50 wt %, represent the prior art. Especiallydue to the high haze value (which characterizes the large-anglescattering), the press plates appear translucent to opaque. The examplesaccording to the invention have a considerably better transparency,which features a substantially lower scattering. The test andcomparative samples prove the effect of particle sizes of the graftcopolymers on the transparency of the PVC articles made therefrom.

The Examples 8 to 12 according to the invention have a highertransparency than the Comparative Examples 1 to 3, which arecross-linked in the same manner and which have particle sizes of above170 nm. When the graft base and the graft shell are cross-linked, thetransparency of a press plate made therefrom will be improvedsubstantially by reducing the particle size to below 200 nm.

Blends consisting of the graft copolymers according to the inventionthat differ from each other in their PBA content (see Blend Example 1)have a higher transparency than Comparative Examples 1 to 4.

In contrast to this, blends of a transparent graft copolymer with S-PVCare opaque. For example, a transparent press plate made from the graftcopolymer of Example 1, which is per se transparent, becomes opaque ifS-PVC is admixed to the graft copolymer to a proportion of 25 wt %.

1-17. (canceled)
 18. A method of preparing a vinyl chloride graftcopolymer composition, the method comprising: forming a vinyl chloridegraft copolymer by: preparing a graft base by polymerizing monomers,wherein the graft base has a first glass transition temperature;grafting a copolymer phase having a second glass transition temperatureonto the graft base by emulsion polymerization, to form a vinyl chloridegraft copolymer latex including the vinyl chloride graft copolymer; andseparating the vinyl chloride graft copolymer as a solid from the vinylgraft copolymer latex, wherein the first glass transition temperature islower than the second glass transition temperature and the averageparticle size of the vinyl chloride graft copolymer is less than 200 nm.19. The method of claim 18, wherein the second glass transitiontemperature is from about 20° C. to about 120° C. and the first glasstransition temperature is from about −80° C. to about 20° C.
 20. Themethod of claim 18, wherein the copolymer phase is grafted onto thegraft base by emulsion polymerization using at least one emulsifier. 21.The method of claim 20, wherein from about 60 wt. % to about 100 wt. %of the at least one emulsifier is pre-charged.
 22. The method of claim18, wherein the graft base of monomers is polymerized at a temperatureof from about 20° C. to about 90° C.
 23. The method of claim 18, whereinthe copolymer phase is grafted onto the graft base at a temperature offrom about 45° C. to about 90° C.
 24. The method of claim 18, whereinthe vinyl chloride graft copolymer comprises from about 5 wt. % to about70 wt. % of the graft base and from about 30 wt. % to about 95 wt. % ofthe copolymer phase.
 25. The method of claim 18, wherein the graft basecomprises a first polymerized vinyl compound and a second polymerizedvinyl compound.
 26. The method of claim 18, wherein the copolymer phasecomprises from about 60 wt. % to about 100 wt. % vinyl chloride and fromabout 0 wt. % to about 40 wt. % polymerized vinyl compounds.
 27. Themethod of claim 18, wherein the graft base and the grafted copolymerphase are cross-linked.
 28. The method of claim 18 and furthercomprising: forming a second vinyl chloride graft copolymer by: graftingthe copolymer onto the graft base by emulsion polymerization to form asecond vinyl chloride graft copolymer latex including the second vinylchloride graft copolymer; and separating the second vinyl chloride graftcopolymer as a solid from the second vinyl graft copolymer latex; andcombining the vinyl chloride graft copolymer and the second vinylchloride graft copolymer, wherein the weight ratio of the graft base tothe grafted copolymer base of the vinyl chloride graft copolymer isdifferent than that of the second vinyl chloride graft copolymer. 29.The method of claim 18, wherein the vinyl chloride graft copolymercomposition has at a transmittance of at least 65%.
 30. The method ofclaim 18, wherein the vinyl chloride graft copolymer composition has ata haze value of less than
 60. 31. A vinyl chloride graft copolymercomposition comprising: a vinyl chloride graft copolymer comprising: apolymerized graft base having a first glass transition temperature; anda copolymer phase grafted onto the graft base, the copolymer phasehaving a second glass transition temperature that is higher than thefirst glass transition temperature, wherein the average particle size ofthe vinyl chloride graft copolymer is less than 200 nm.
 32. The vinylchloride graft copolymer composition of claim 31, further comprising asecond vinyl graft chloride wherein the vinyl chloride graft copolymerand the second copolymer are selected from the group consisting of:graft copolymer A including from about 41 wt. % to about 70 wt. % of thegraft base and from about 30 wt. % to about 59 wt. % of the graftedcopolymer phase; graft copolymer B including from about 26 wt. % toabout 40 wt. % of the graft base and from about 60 wt. % to about 74 wt.% of the grafted copolymer phase; and graft copolymer C including fromabout 5 wt. % to about 25 wt. % of the graft base and from about 75 wt.% to about 95 wt. % of the grafted copolymer phase.
 33. The vinylchloride graft copolymer composition of claim 31, further comprising asecond vinyl graft chloride wherein the vinyl chloride graft copolymerand the second copolymer are selected from the group consisting of: fromabout 1.0 wt. % to about 99 wt. % graft copolymer A; from about 1.0 wt.% to about 99 wt. % graft copolymer B; and from about 1.0 wt. % to about99 wt. % graft copolymer C; wherein the graft base has a glasstransition temperature from about −80° C. to about 20° C., the graftedcopolymer phase has a glass transition temperature from about 20° C. toabout 120° C. and the vinyl chloride graft copolymer compositioncontains at least 25 wt. % of the graft base, and the balance is thegrafted copolymer phase.
 34. The vinyl chloride graft copolymercomposition of claim 31, wherein the vinyl chloride graft copolymercomposition has at a transmittance of at least 65%.
 35. The vinylchloride graft copolymer composition of claim 31, wherein the vinylchloride graft copolymer composition has at a haze value of less than60.
 36. The vinyl chloride graft copolymer composition of claim 31,further comprising a second vinyl graft chloride wherein the vinylchloride graft copolymer has a first weight ratio of grafted base tografted copolymer phase and the second vinyl chloride graft copolymerhas a second weight ratio of graft base to grafted copolymer phase.